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Rita M. Cantor

University of California System

68H指数
235论文数
3.9W被引数
收录论文 69
发表时间
Genome-wide mapping of brain phenotypes in extended pedigrees with strong genetic loading for bipolar disorder
err2020-06-30
err4
PREAI
errFears, Scott C.; Service, Susan K.; Kremeyer, Barbara; Araya, Carmen; Araya, Xinia; Bejarano, Julio; Ramirez, Margarita; Castrillon, Gabriel; Gomez-Franco, Juliana; Lopez, Maria C.; Montoya, Gabriel; Montoya, Patricia; Aldana, Ileana; Teshiba, Terri M.; Al-Sharif, Noor B.; Jalbrzikowski, Maria; Tishler, Todd A.; Escobar, Javier; Ruiz-Linares, Andres; Lopez-Jaramillo, Carlos; Macaya, Gabriel; Molina, Julio; Reus, Victor, I; Cantor, Rita M.; Sabatti, Chiara; Freimer, Nelson B.; Bearden, Carrie E.
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Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates
err2020-02-24
err25
errOAAI
errSul, Jae Hoon; Service, Susan K.; Huang, Alden Y.; Ramensky, Vasily; Hwang, Sun-Goo; Teshiba, Terri M.; Park, YoungJun; Ori, Anil P. S.; Zhang, Zhongyang; Mullins, Niamh; Olde Loohuis, Loes; Fears, Scott C.; Araya, Carmen; Araya, Xinia; Spesny, Mitzi; Bejarano, Julio; Ramirez, Margarita; Castrillon, Gabriel; Gomez-Makhinson, Juliana; Lopez, Maria C.; Montoya, Gabriel; Montoya, Claudia P.; Aldana, Ileana; Escobar, Javier I.; Ospina-Duque, Jorge; Kremeyer, Barbara; Bedoya, Gabriel; Ruiz-Linares, Andres; Cantor, Rita M.; Molina, Julio; Coppola, Giovanni; Ophoff, Roel A.; Macaya, Gabriel; Lopez-Jaramillo, Carlos; Reus, Victor; Bearden, Carrie E.; Sabatti, Chiara; Freimer, Nelson B.
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Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
err2019-10-24
err87
errOAAI
errGallagher, C. S.; Makinen, N.; Harris, H. R.; Rahmioglu, N.; Uimari, O.; Cook, J. P.; Shigesi, N.; Ferreira, T.; Velez-Edwards, D. R.; Edwards, T. L.; Mortlock, S.; Ruhioglu, Z.; Day, F.; Becker, C. M.; Karhunen, V.; Martikainen, H.; Jarvelin, M. -R.; Cantor, R. M.; Ridker, P. M.; Terry, K. L.; Buring, J. E.; Gordon, S. D.; Medland, S. E.; Montgomery, G. W.; Nyholt, D. R.; Hinds, D. A.; Tung, J. Y.; Perry, J. R. B.; Lind, P. A.; Painter, J. N.; Martin, N. G.; Morris, A. P.; Chasman, D. I.; Missmer, S. A.; Zondervan, K. T.; Morton, C. C.; Agee, Michelle; Alipanahi, Babak; Auton, Adam; Bell, Robert K.; Bryc, Katarzyna; Elson, Sarah L.; Fontanillas, Pierre; Furlotte, Nicholas A.; Huber, Karen E.; Kleinman, Aaron; Litterman, Nadia K.; McIntyre, Matthew H.; Mountain, Joanna L.; Noblin, Elizabeth S.; Northover, Carrie A. M.; Pitts, Steven J.; Sathirapongsasuti, J. Fah; Sazonova, Olga V.; Shelton, Janie F.; Shringarpure, Suyash; Tian, Chao; Vacic, Vladimir; Wilson, Catherine H.
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Integration of human adipocyte chromosomal interactions with adipose gene expression prioritizes obesity-related genes from GWAS (vol 9, 1512, 2018)
err2018-08-22
err4
errOAAI
errPan, David Z.; Garske, Kristina M.; Alvarez, Marcus; Bhagat, Yash V.; Boocock, James; Nikkola, Elina; Miao, Zong; Raulerson, Chelsea K.; Cantor, Rita M.; Civelek, Mete; Glastonbury, Craig A.; Small, Kerrin S.; Boehnke, Michael; Lusis, Aldons J.; Sinsheimer, Janet S.; Mohlke, Karen L.; Laakso, Markku; Pajukanta, Paivi; Ko, Arthur
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DMD genotype correlations from the Duchenne Registry: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation subtype
err2018-07-12
err68
errOAAI
errWang, Richard T.; Barthelemy, Florian; Martin, Ann S.; Douine, Emilie D.; Eskin, Ascia; Lucas, Ann; Lavigne, Jenifer; Peay, Holly; Khanlou, Negar; Sweeney, Lee; Cantor, Rita M.; Miceli, M. Carrie; Nelson, Stanley F.
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Repurposing Dantrolene for Long-Term Combination Therapy to Potentiate Antisense-Mediated DMD Exon Skipping in the mdx Mouse
err2018-06-01
err10
errOAAI
errWang, Derek W.; Mokhonova, Ekaterina I.; Kendall, Genevieve C.; Becerra, Diana; Naeini, Yalda B.; Cantor, Rita M.; Spencer, Melissa J.; Nelson, Stanley F.; Miceli, M. Carrie
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Integration of human adipocyte chromosomal interactions with adipose gene expression prioritizes obesity-related genes from GWAS
err2018-04-17
err67
errOAAI
errPan, David Z.; Garske, Kristina M.; Alvarez, Marcus; Bhagat, Yash V.; Boocock, James; Nikkola, Elina; Miao, Zong; Raulerson, Chelsea K.; Cantor, Rita M.; Civelek, Mete; Glastonbury, Craig A.; Small, Kerrin S.; Boehnke, Michael; Lusis, Aldons J.; Sinsheimer, Janet S.; Mohlke, Karen L.; Laakso, Markku; Pajukanta, Paivi; Ko, Arthur
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Family-specific aggregation of lipid GWAS variants confers the susceptibility to familial hypercholesterolemia in a large Austrian family脂质ghis变体的家族特异性聚集使奥地利大家族对家族性高胆固醇血症的易感性
err2017-09-01
err8
errOAAI
errNikkola, Elina; Ko, Arthur; Alvarez, Marcus; Cantor, Rita M.; Garske, Kristina; Kim, Elliot; Gee, Stephanie; Rodriguez, Alejandra; Muxel, Reinhard; Matikainen, Niina; Soderlund, Sanni; Motazacker, Mahdi M.; Boren, Jan; Lamina, Claudia; Kronenberg, Florian; Schneider, Wolfgang J.; Palotie, Aarno; Laakso, Markku; Taskinen, Marja-Riitta; Pajukanta, Paivi
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ASD restricted and repetitive behaviors associated at 17q21.33: genes prioritized by expression in fetal brains
err2017-05-23
err14
errOAAI
errCantor, R. M.; Navarro, L.; Won, H.; Walker, R. L.; Lowe, J. K.; Geschwind, D. H.
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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects来自41,321受试者的全基因组研究的拷贝数变异对精神分裂症的贡献
err2016-11-21
err753
errOAAI
errMarshall, Christian R.; Howrigan, Daniel P.; Merico, Daniele; Thiruvahindrapuram, Bhooma; Wu, Wenting; Greer, Douglas S.; Antaki, Danny; Shetty, Aniket; Holmans, Peter A.; Pinto, Dalila; Gujral, Madhusudan; Brandler, William M.; Malhotra, Dheeraj; Wang, Zhouzhi; Fajarado, Karin V. Fuentes; Maile, Michelle S.; Ripke, Stephan; Agartz, Ingrid; Albus, Margot; Alexander, Madeline; Amin, Farooq; Atkins, Joshua; Bacanu, Silviu A.; Belliveau, Richard A., Jr.; Bergen, Sarah E.; Ertalan, Marcelo; Bevilacqua, Elizabeth; Bigdeli, Tim B.; Black, Donald W.; Bruggeman, Richard; Buccola, Nancy G.; Buckner, Randy L.; Bulik-Sullivan, Brendan; Byerley, William; Cahn, Wiepke; Cai, Guiqing; Cairns, Murray J.; Campion, Dominique; Cantor, Rita M.; Carr, Vaughan J.; Carrera, Noa; Catts, Stanley V.; Chambert, Kimberley D.; Cheng, Wei; Cloninger, C. Robert; Cohen, David; Cormican, Paul; Craddock, Nick; Crespo-Facorro, Benedicto; Crowley, James J.; Curtis, David; Davidson, Michael; Davis, Kenneth L.; Degenhardt, Franziska; Del Favero, Jurgen; DeLisi, Lynn E.; Dikeos, Dimitris; Dinan, Timothy; Djurovic, Srdjan; Donohoe, Gary; Drapeau, Elodie; Duan, Jubao; Dudbridge, Frank; Eichhammer, Peter; Eriksson, Johan; Escott-Price, Valentina; Essioux, Laurent; Fanous, Ayman H.; Farh, Kai-How; Farrell, Martilias S.; Frank, Josef; Franke, Lude; Freedman, Robert; Freimer, Nelson B.; Friedman, Joseph I.; Forstner, Andreas J.; Fromer, Menachem; Genovese, Giulio; Georgieva, Lyudmila; Gershon, Elliot S.; Giegling, Ina; Giusti-Rodriguez, Paola; Godard, Stephanie; Goldstein, Jacqueline I.; Gratten, Jacob; de Haan, Lieuwe; Hamshere, Marian L.; Hansen, Mark; Hansen, Thomas; Haroutunian, Vahram; Hartmann, Annette M.; Henskens, Frans A.; Herms, Stefan; Hirschhorn, Joel N.; Hoffinann, Per; Hofman, Andrea; Huang, Hailiang; Ikeda, Masashi; Joa, Inge; Kahler, Anna K.; Kahn, Rene S.; Kalaydjieva, Luba; Karjalainen, Juha; Kavanagh, David; Keller, Matthew C.; Kelly, Brian J.; Kennedy, James L.; Kim, Yunjung; Knowles, James A.; Konte, Bettina; Laurent, Claudine; Lee, Phil; Lee, S. Hong; Legge, Sophie E.; Lerer, Bernard; Levy, Deborah L.; Liang, Kung-Yee; Lieberman, Jeffrey; Lonnqvist, Jouko; Loughland, Carmel M.; Magnusson, Patrik K. E.; Maher, Brion S.; Maier, Wolfgang; Mallet, Jacques; Mattheisen, Manuel; Mattingsdal, Morten; McCarley, Robert W.; McDonald, Colm; McIntosh, Andrew M.; Meier, Sandra; Meijer, Carin J.; Melle, Ingrid; Mesholam-Gately, Raquelle I.; Metspalu, Andres; Michie, Patricia T.; Milani, Lili; Milanova, Vihra; Mokrab, Younes; Morris, Derek W.; Muller-Myhsok, Bertram; Murphy, Kieran C.; Murray, Robin M.; Myin-Germeys, Inez; Nenadic, Igor; Nertney, Deborah A.; Nestadt, Gerald; Nicodemus, Kristin K.; Nisenbaum, Laura; Nordin, Annelie; O'Callaghan, Eadbhard; O'Dushlaine, Colm; Oh, Sang-Yun; Olincy, Ann; Olsen, Line; O'Neill, F. Anthony; Van Os, Jim; Pantelis, Christos; Papadimitriou, George N.; Parkhomenko, Elena; Pato, Michele T.; Paunio, Tiina; Perkins, Diana O.; Pers, Tune H.; Pietilainen, Olli; Pimm, Jonathan; Pocklington, Andrew J.; Powell, John; Price, Alkes; Pulver, Ann E.; Purcell, Shaun M.; Quested, Digby; Rasmussen, Henrik B.; Reichenberg, Abraham; Reimers, Mark A.; Richards, Alexander L.; Roffman, Joshua L.; Roussos, Panos; Ruderfer, Douglas M.; Salomaa, Veikko; Sanders, Alan R.; Savitz, Adam; Schall, Ulrich; Schulze, Thomas G.; Schwab, Sibylle G.; Scolnick, Edward M.; Scott, Rodney J.; Seidman, Larry J.; Shi, Jianxin; Silverman, Jeremy M.; Smoller, Jordan W.; Soderman, Erik; Spencer, Chris C. A.; Stahl, Eli A.; Strengman, Eric; Strohmaier, Jana; Stroup, T. Scott; Suvisaari, Jaana; Svrakic, Dragan M.; Szatkiewicz, Jin P.; Thirumalai, Srinivas; Tooney, Paul A.; Veijola, Juha; Visscher, Peter M.; Waddington, John; Walsh, Dermot; Webb, Bradley T.; Weiser, Mark; Wildenauer, Dieter B.; Williams, Nigel M.; Williams, Stephanie; Witt, Stephanie H.; Wolen, Aaron R.; Wormley, Brandon K.; Wray, Naomi R.; Wu, Jing Qin; Zai, Clement C.; Adolfsson, Rolf; Andreassen, Ole A.; Blackwood, Douglas H. R.; Bramon, Elvira; Buxbaum, Joseph D.; Cichon, Sven; Collier, David A.; Corvin, Aiden; Daly, Mark J.; Darvasi, Ariel; Domenici, Enrico; Esko, Tonu; Gejman, Pablo V.; Gill, Michael; Gurling, Hugh; Hultman, Christina M.; Iwata, Nakao; Jablensky, Assen V.; Jonsson, Erik G.; Kendler, Kenneth S.; Kirov, George; Knight, Jo; Levinson, Douglas F.; Li, Qingqin S.; McCarroll, Steven A.; McQuillin, Andrew; Moran, Jennifer L.; Mowry, Bryan J.; Nothen, Markus M.; Ophoff, Roel A.; Owen, Michael J.; Palotie, Aarno; Pato, Carlos N.; Petryshen, Tracey L.; Posthuma, Danielle; Rietschel, Marcella; Riley, Brien P.; Rujescu, Dan; Sklar, Pamela; St Clair, David; Walters, James T. R.; Werge, Thomas; Siillivan, Patrick F.; O'Donovan, Michael C.; Scherer, Stephen W.; Neale, Benjamin M.; Sebat, Jonathan
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Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families
err2016-09-01
err154
errOAAI
errLeppa, Virpi M.; Kravitz, Stephanie N.; Martin, Christa Lese; Andrieux, Joris; Le Caignec, Cedric; Martin-Coignard, Dominique; DyBuncio, Christina; Sanders, Stephan J.; Lowe, Jennifer K.; Cantor, Rita M.; Geschwind, Daniel H.
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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci从71个风险位点洞察自闭症谱系障碍基因组结构和生物学
errNEURON
IF15
err2015-09-01
err1.1K
errOAAI
errSanders, Stephan J.; Xin He; Willsey, A. Jeremy; Ercan-Sencicek, A. Gulhan; Samocha, Kaitlin E.; Cicek, A. Ercument; Murtha, Michael T.; Bal, Vanessa H.; Bishop, Somer L.; Shan Dong; Goldberg, Arthur P.; Cai Jinlu; Keaney, John F., III; Klei, Lambertus; Mandell, Jeffrey D.; Moreno-De-Luca, Daniel; Poultney, Christopher S.; Robinson, Elise B.; Smith, Louw; Solli-Nowlan, Tor; Su, Mack Y.; Teran, Nicole A.; Walker, Michael F.; Werling, Donna M.; Beaudet, Arthur L.; Cantor, Rita M.; Fombonne, Eric; Geschwind, Daniel H.; Grice, Dorothy E.; Lord, Catherine; Lowe, Jennifer K.; Mane, Shrikant M.; Martin, Donna M.; Morrow, Eric M.; Talkowski, Michael E.; Sutcliffe, James S.; Walsh, Christopher A.; Yu, Timothy W.; Ledbetter, David H.; Martin, Christa Lese; Cook, Edwin H.; Buxbaum, Joseph D.; Daly, Mark J.; Devlin, Bernie; Roeder, Kathryn; State, Matthew W.
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Social Responsiveness, an Autism Endophenotype: Genomewide Significant Linkage to Two Regions on Chromosome 8
err2015-03-01
err44
errOAAI
errLowe, Jennifer K.; Werling, Donna M.; Constantino, John N.; Cantor, Rita M.; Geschwind, Daniel H.
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Amerindian-specific regions under positive selection harbour new lipid variants in Latinos
err2014-06-02
err78
errOAAI
errKo, Arthur; Cantor, Rita M.; Weissglas-Volkov, Daphna; Nikkola, Elina; Reddy, Prasad M. V. Linga; Sinsheimer, Janet S.; Pasaniuc, Bogdan; Brown, Robert; Alvarez, Marcus; Rodriguez, Alejandra; Rodriguez-Guillen, Rosario; Bautista, Ivette C.; Arellano-Campos, Olimpia; Munoz-Hernandez, Linda L.; Salomaa, Veikko; Kaprio, Jaakko; Jula, Antti; Jauhiainen, Matti; Heliovaara, Markku; Raitakari, Olli; Lehtimaki, Terho; Eriksson, Johan G.; Perola, Markus; Lohmueller, Kirk E.; Matikainen, Niina; Taskinen, Marja-Riitta; Rodriguez-Torres, Maribel; Riba, Laura; Tusie-Luna, Teresa; Aguilar-Salinas, Carlos A.; Pajukanta, Paeivi
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Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder
err2014-02-17
err32
errOAAI
errWerling, Donna M.; Lowe, Jennifer K.; Luo, Rui; Cantor, Rita M.; Geschwind, Daniel H.
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Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci
err2013-03-15
err116
errOAAI
errWeissglas-Volkov, Daphna; Aguilar-Salinas, Carlos A.; Nikkola, Elina; Deere, Kerry A.; Cruz-Bautista, Ivette; Arellano-Campos, Olimpia; Liliana Munoz-Hernandez, Linda; Gomez-Munguia, Lizeth; Luisa Ordonez-Sanchez, Maria; Reddy, Prasad M. V. Linga; Lusis, Aldons J.; Matikainen, Niina; Taskinen, Marja-Riitta; Riba, Laura; Cantor, Rita M.; Sinsheimer, Janet S.; Tusie-Luna, Teresa; Pajukanta, Paeivi
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Fine mapping of Xq28: both MECP2 and IRAK1 contribute to risk for systemic lupus erythematosus in multiple ancestral groups
err2013-03-01
err91
errOAAI
errKaufman, Kenneth M.; Zhao, Jian; Kelly, Jennifer A.; Hughes, Travis; Adler, Adam; Sanchez, Elena; Ojwang, Joshua O.; Langefeld, Carl D.; Ziegler, Julie T.; Williams, Adrienne H.; Comeau, Mary E.; Marion, Miranda C.; Glenn, Stuart B.; Cantor, Rita M.; Grossman, Jennifer M.; Hahn, Bevra H.; Song, Yeong Wook; Yu, Chack-Yung; James, Judith A.; Guthridge, Joel M.; Brown, Elizabeth E.; Alarcon, Graciela S.; Kimberly, Robert P.; Edberg, Jeffrey C.; Ramsey-Goldman, Rosalind; Petri, Michelle A.; Reveille, John D.; Vila, Luis M.; Anaya, Juan-Manuel; Boackle, Susan A.; Stevens, Anne M.; Freedman, Barry I.; Criswell, Lindsey A.; Pons-Estel, Bernardo A.; Lee, Joo-Hyun; Lee, Ji-Seon; Chang, Deh-Ming; Scofield, R. Hal A.; Gilkeson, Gary S.; Merrill, Joan T.; Niewold, Timothy B.; Vyse, Timothy James; Bae, Sang-Cheol; Alarcon-Riquelme, Marta E.; Jacob, Chaim O.; Sivils, Kathy Moser; Gaffney, Patrick M.; Harley, John B.; Sawalha, Amr H.; Tsao, Betty P.
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Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid
err2013-01-15
err51
errOAAI
errLuykx, J. J.; Bakker, S. C.; Lentjes, E.; Neeleman, M.; Strengman, E.; Mentink, L.; DeYoung, J.; de Jong, S.; Sul, J. H.; Eskin, E.; van Eijk, K.; van Setten, J.; Buizer-Voskamp, J. E.; Cantor, R. M.; Lu, A.; van Amerongen, M.; van Dongen, E. P. A.; Keijzers, P.; Kappen, T.; Borgdorff, P.; Bruins, P.; Derks, E. M.; Kahn, R. S.; Ophoff, R. A.
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Systems Biology of the Vervet Monkey
err2013-01-01
err91
errOAAI
errJasinska, Anna J.; Schmitt, Christopher A.; Service, Susan K.; Cantor, Rita M.; Dewar, Ken; Jentsch, James D.; Kaplan, Jay R.; Turner, Trudy R.; Warren, Wesley C.; Weinstock, George M.; Woods, Roger P.; Freimer, Nelson B.
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Support for calcium channel gene defects in autism spectrum disorders
err2012-12-15
err72
errOAAI
errLu, Ake Tzu-Hui; Dai, Xiaoxian; Martinez-Agosto, Julian A.; Cantor, Rita M.
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